Mechanism for the decomposition of lithium borohydride

TL;DR

This study uses first-principles calculations to propose a defect-mediated mechanism for lithium borohydride decomposition, highlighting the role of native defects and their migration in hydrogen release processes.

Contribution

It introduces a detailed defect-based mechanism for LiBH₄ decomposition, emphasizing the role of native defects and their migration pathways.

Findings

Hydrogen interstitials (H_i^-) are key in nucleating LiH formation.

Lithium vacancies and interstitials are highly mobile and influence charge neutrality.

H_i^- diffusion is the rate-limiting step in decomposition.

Abstract

We report first-principles density functional theory studies of native defects in lithium borohydride (LiBH$_{4}$), a potential material for hydrogen storage. Based on our detailed analysis of the structure, energetics, and migration of lithium-, boron-, and hydrogen-related defects, we propose a specific mechanism for the decomposition and dehydrogenation of LiBH$_{4}$ that involves mass transport mediated by native defects. In this mechanism, LiBH$_{4}$ releases borane (BH$_{3}$) at the surface or interface, leaving the negatively charged hydrogen interstitial (H$_{i}^{-}$) in the material, which then acts as the nucleation site for LiH formation. The diffusion of H$_{i}^{-}$ in the bulk LiBH$_{4}$ is the rate-limiting step in the decomposition kinetics. Lithium vacancies and interstitials have low formation energies and are highly mobile. These defects are responsible for maintaining local charge neutrality as other charged defects migrating along the material, and assisting in the formation of LiH. In light of this mechanism, we discuss the effects of metal additives on hydrogen desorption kinetics.